Evaluating the Effect of Cryptorchidism on Clinical Stage of Testicular Seminoma

Xingyuan Wang; Zeyu Chen; Shi Qiu; Dehong Cao; Kun Jin; Jin Li; Bo Chen; Yin Huang; Yige Bao; Liangren Liu; Qiang Wei

doi:10.2147/CMAR.S236618

Evaluating the Effect of Cryptorchidism on Clinical Stage of Testicular Seminoma

Cancer Manag Res. 2020 Jun 23:12:4883-4888. doi: 10.2147/CMAR.S236618. eCollection 2020.

Authors

Xingyuan Wang^#^{1

2}, Zeyu Chen^#^{1

2}, Shi Qiu^#^{1

3}, Dehong Cao¹, Kun Jin^{1

2}, Jin Li^{1

2}, Bo Chen^{1

2}, Yin Huang^{1

2}, Yige Bao¹, Liangren Liu¹, Qiang Wei¹

Affiliations

¹ Department of Urology/Institute of Urology, West China Hospital, Sichuan University, Chengdu 610041, People's Republic of China.
² West China School of Medicine, Sichuan University, Chengdu, People's Republic of China.
³ Center of Biomedical Big Data, West China Hospital, Sichuan University, Chengdu, Sichuan, People's Republic of China.

^# Contributed equally.

Abstract

Objective: To study the effect of cryptorchidism on clinical stage (CS) of testicular seminoma (TS).

Patients and methods: In the Surveillance Epidemiology and End Results (SEER) database (2006-2016), people with TS were enrolled in our research. Multivariable logistic regression models were constructed to compare the impact of cryptorchidism on CS.

Results: This research was based on the registry information of 12,991 TS patients. All patients with a median age of 36 (13-107) years were pathologically diagnosed with orchiectomy or needle biopsy specimens. Patients with CS I, II, and III TS accounted for 70.68% (n = 9182), 8.30% (n = 1078), and 5.75% (n = 747) of all patients, respectively; still there were 15.27% (n = 1984) of patients whose CS could not be identified or was not available. Among all included patients, 43.45% (n = 5644) of them had normal testis, 2.93% (n = 272) had cryptorchidism, and the primary site of 54.46% (n = 7075) of patients' testis was unavailable. According to our study, patients with cryptorchidism were more likely to suffer advanced CS [OR=1.14, 95% CI (1.01-1.28), p=0.0407]. Furthermore, this effect became more remarkable after adjusting for other factors including age, region, marital status, race, year of diagnosis and laterality [OR=1.23, 95% CI (1.13-1.32), p<0.0001].

Conclusion: According to this study, TS patients with cryptorchidism would be at a higher risk of suffering advanced cancer than patients with normal testis. It demonstrates that surgical correction for cryptorchidism should be timely, and specific management should be conducted on this kind of TS patients.

Keywords: clinical stage; cryptorchidism; testicular seminoma.